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Investigative Ophthalmology & Visual Science|March 13, 2012
Tyrosine-mutant AAV8 delivery of human MERTK provides long-term retinal preservation in RCS ratsWen-Tao Deng, Astra Dinculescu, Qiuhong Li, et al.Plos One|February 17, 2016
AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene TherapyAstra Dinculescu, Rachel M Stupay, Wen-Tao Deng, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|November 4, 2010
Novel properties of tyrosine-mutant AAV2 vectors in the mouse retinaHilda Petrs-Silva, Astra Dinculescu, Qiuhong Li, et al.Human Gene Therapy|December 7, 2011
Gene therapy for retinitis pigmentosa caused by MFRP mutations: human phenotype and preliminary proof of conceptAstra Dinculescu, Jackie Estreicher, Juan C Zenteno, et al.Pageof 4